CombiBreed Health Chat UPDATED

CombiBreed Health Chat UPDATED

Commandez l'examen

99,95

82,60 (hors 21% TVA)

Description

Espèce cible et races

Chat

Toutes les races

Prélèvement

Ecouvillon génétique
EDTA sang complet

Délai

21 jours

Catégorie

Génétique, bilans

Code

K5500

Analyses

Adrenal hyperplasia

CYP11B1 G>A

Alpha-Mannosidosis

Alpha-Mannosidosis

FASLG c.413_414insA

Cystinuria Type B

Cystinuria Type B variant 1

SLC7A9 c.706G>A

Cystinuria Type B variant 2

SLC7A9 c.881T>A

Cystinuria Type B variant 3

SLC7A9 c.1175C>T

Dihydropyrimidinase deficiency

DPYS c.1303G>A

Factor XI deficiency

F11 c.1546G>A

Factor XII deficiency

F12 c.1631G>C

Frontonasal dysplasia

ALX1 c.496del

11-1 Gangliosidosis GM1

c.1448G>C

Gangliosidosis GM2A type II

GM2A delGGTC

Gangliosidosis GM2 type II - 1

HEXB delC

Gangliosidosis GM2 type II - 2

HEXB c.667C>T

Gangliosidosis GM2 type II - 3

HEXB c.1467_91inv25

Gangliosidosis GM2 type II - 4

HEXB c.1244_1250del

Glycogen storage disease IV

GBE1 2xIVS+

Haemophilia B 1

F9 c.383G>A

Haemophilia B 2

F9 c.1150C>T

19-1 Hypertrophic cardiomyopathy 1

MYBPC3 A31P

19-2 Hypertrophic cardiomyopathy 3

MYBPC3 R820W

Hypokalemic periodic paralysis

WNK4 2899

Hypotrichosis, short life

FOXN1 c.1030_3del

Mucopolysaccharidosis I

IDUA 3bp del

Mucopolysaccharidosis VI

ARSB c.1427T>C

Mucopolysaccharidosis VII

Mucopolysaccharidosis VII 1

GUSB c.1074G>A

25-1 Mucopolysaccharidosis VII 2

GUSB c.1423T>G

25-2 Mucopolysaccharidosis VII 3

GUSB c.1426C>T

Congenital Myasthenic Syndrome

COLQ c.1190G>A

Myotonia congenita

Myotonia congenita variant 1

CLCN1 c.1930+1G>T

Myotonia congenita variant 2

CLCN1 8bp del

Myotonia congenita variant 3

CLCN1 c.991G>C

Niemann-Pick Syndroom C1 - 1

NPC1 c.2864G>C

Multidrug resistance 1

ABCB1 c.1930_1del

Niemann-Pick Syndrome C1 - 2

NPC1 c.1322A>C

Osteochondrodysplasia

TRPV4 c.1024G>T

34-1 Polycystic kidney disease 1

PKD1 c.10063>A

Primary hyperoxaluria type II

GRHPR G>A

35-1 Pyruvate kinase deficiency

PKLR c.707-53G>A

CEP290 IVS50+9T>G

Rod-cone dysplasia

CRX 546

KIF3B c.1000G>A

Spinal muscular atrophy

LIX1 140kbdel

Vit D-deficiency rickets I

CYP27B1 c.637G>T

Type sanguin allèle b

CMAH 139/-53

Type sanguin allèle aAB

Type sanguin allèle aAB 1

CMAH c.364C>T

Bloedgroep aAB allel 2

CMAH c.1322del

44-1 Couleur robe A-locus (Agouti)

ASIP

Colour robe A-locus (Charcoal)

ASIP

45-1 Couleur robe B-Locus Chocolade

45-2 Couleur robe B-Locus Cinnamon

45-3 Couleur robe C-locus (Burmese)

45-4 Couleur robe C-Locus (Siamois)

45-5 Couleur robe D-locus Dilution

Couleur robe E-locus (Ambre)

MC1R

46-1 Couleur robe E-locus (Russet)

46-2 Couleur robe Gold (Copper)

CORIN c.2425C>T

46-3 Couleur robe Gold (Sunshine)

CORIN c.2383C>T

46-4 Couleur robe Gold (Extreme)

CORIN c.839G>A

46-5 Motif robe Tabby

46-6 CombiBreed Longueur du poil

46-7 Longueur poil Ragdoll

FGF5 c.356_7insT

46-8 Longueur poil Norvégien

FGF5 c.406C>T

46-9 Longueur poil Ragdoll/M. Coone

FGF5 c.474del

Haarlengte Maine Coon

FGF c.474del

Longueur du poil toutes races

FGF5 c.475A>C

48-1 Poil frissé Cornish Rex

LPAR6

48-2 Poil Devon Rex et Sphynx

KRT71

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